NAGA, also known as alpha-N-acetylgalactosaminidase and alpha-galactosidase B, is a member of the glycosyl hydrolase 27 family. NAGA plays an important role in the breakdown of glycolipids by removing the terminal alpha-N-acetylgalactosamine residues from glycolipids and glycopeptides. Additionally, NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase. Defects in the NAGA gene have been identified as the cause of Schindler type I and type II disease.
![Western Blot alpha-N-acetylgalactosaminidase/NAGA Antibody [Unconjugated]](http://images.novusbio.com/fullsize2/alphaNacetylgalactosaminidase_AF6717_Western_Blot_13878.jpg)
